Description

Peramivir is a potent and selective neuraminidase inhibitor used as an antiviral agent. This compound is critical for the research and development of treatments targeting influenza viruses, including pandemic strains. It is primarily utilized by pharmaceutical manufacturers, research institutions, and contract development organizations engaged in antiviral drug discovery and production.

Application

• Active Pharmaceutical Ingredient (API) for the formulation of injectable antiviral medications.
• Reference Standard in analytical laboratories for quality control and method validation of peramivir-based products.
• Biochemical Research for studying the mechanism of neuraminidase inhibition and influenza virus replication.
• Preclinical and Clinical Development of new anti-influenza therapeutics and combination therapies.
• Process Chemistry for the development and scale-up of synthetic routes for peramivir manufacturing.

Basic Information

Product Name	Peramivir
CAS No.	330600-85-6
Molecular Formula	C15H28N4O4
Molecular Weight	328.41 g/mol
Synonyms	(1S,2S,3R,4R)-3-[(1S)-1-Acetamido-2-ethylbutyl]-4-(diaminomethylideneamino)-2-hydroxycyclopentane-1-carboxylic acid; BCX-1812; RWJ-270201; Peramivir Trihydrate; Rapiacta; Peramivirum; Peramivir Anhydrous
EINECS	Contact for details

Quality Control

Our Peramivir is manufactured under strict quality systems to ensure it meets the rigorous standards required for pharmaceutical applications. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We support compliance with cGMP, ICH Q7, and other relevant pharmacopeial guidelines.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under dry conditions to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	≥98.0%
Water Content (KF)	≤2.0%
Residue on Ignition	≤0.1%
Heavy Metals	≤20 ppm
Related Substances (HPLC)	Individual impurity ≤0.5%; Total impurities ≤2.0%
Microbial Limits	Meets Ph. Eur. 2.6.12 / USP <61> requirements

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.